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2-Hydroxymethyl-4-methoxyphenylboronic acid is a boronic acid derivative characterized by the presence of a hydroxymethyl and a methoxy group. This chemical compound is known for its potential applications in organic synthesis and medicinal chemistry, making it a valuable and versatile building block for the synthesis of complex molecules.

762263-92-3

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762263-92-3 Usage

Uses

Used in Organic Synthesis:
2-Hydroxymethyl-4-methoxyphenylboronic acid is used as a building block for the synthesis of complex molecules, owing to its unique structure and properties. It facilitates the formation of boronate esters, which are useful in various organic reactions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Hydroxymethyl-4-methoxyphenylboronic acid is used as a reagent in the development of new pharmaceutical drugs. Its ability to form boronate esters makes it a promising candidate for the synthesis of bioactive compounds with potential therapeutic applications.
Used in Chemical Biology Research:
2-Hydroxymethyl-4-methoxyphenylboronic acid also serves as a valuable tool in chemical biology research. Its unique structure allows for the exploration of novel biochemical pathways and the development of new strategies for targeting specific biological processes.
Overall, the diverse applications of 2-Hydroxymethyl-4-methoxyphenylboronic acid in organic synthesis, medicinal chemistry, and chemical biology research highlight its significance as a versatile chemical compound with great potential in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 762263-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,2,2,6 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 762263-92:
(8*7)+(7*6)+(6*2)+(5*2)+(4*6)+(3*3)+(2*9)+(1*2)=173
173 % 10 = 3
So 762263-92-3 is a valid CAS Registry Number.

762263-92-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-(Hydroxymethyl)-4-methoxyphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [2-(hydroxymethyl)-4-methoxyphenyl]boronic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:762263-92-3 SDS

762263-92-3Downstream Products

762263-92-3Relevant academic research and scientific papers

C5A RECEPTOR ANTAGONISTS

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Page/Page column 147-148, (2008/06/13)

The present invention is related to a compound, preferably a C5a receptor antagonist, having the following structure, Rl, R2, R3, R4, R5, R6, R7, R8, R9, Rl0, RI l, R12, R13, R14, R15, R16, Rl7, R18, Rl9, R20, R21 and R22 are individually and independently selected from the group comprising H, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl, substituted cycloalkyl, heterocyclyl, substituted heterocyclyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, arylalkyl, substituted arylalkyl, heteroarylalkyl, substituted heteroarylalkyl, alkoxyl, substituted alkoxyl, aryloxy, substituted aryloxy, arylalkyloxy, substituted arylalkyloxy, acyloxy, substituted acyloxy, halogen, hydroxyl, nitro, cyano, acyl, substituted acyl, mercapto, alkylthio, substituted alkylthio, amino, substituted amino, alkylamino, substituted alkylamino, bisalkyl amino, substituted bisalkyl amino, cyclic amino, substituted cyclic amino, carbamoyl (-CONH2), substituted carbamoyl, carboxyl, carbamate, alkoxycarbonyl, substituted alkoxycarbonyl, acylamino, substituted acylamino, sulfamoyl (-SO2NH2), substituted sulfamoyl, haloalkyl, haloalkyloxy, -C(O)H, trialkylsilyl and azido.

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